Clinical Research Associate
Prestige Biopharma Group is hiring a Clinical Research Associate in the healthtech sector to manage clinical trial sites. The role involves protocol review, site initiation, ongoing monitoring, and ensuring full regulatory compliance with GCP and ICH guidelines. Candidates are expected to have a background in oncology and strong attention to detail for data integrity. The position requires travel and proficiency in clinical trial management systems.
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Experience
2+ years
Function
Research
Work mode
Onsite, Singapore
Company
Tier 2
What you will work on
Prestige Biopharma Group is hiring a Clinical Research Associate in the healthtech sector to manage clinical trial sites. The role involves protocol review, site initiation, ongoing monitoring, and ensuring full regulatory compliance with GCP and ICH guidelines. Candidates are expected to have a background in oncology and strong attention to detail for data integrity. The position requires travel and proficiency in clinical trial management systems.
TAL's take
Solid mid-level role in the biopharma sector with clearly defined responsibilities and regulatory focus.
Highly specific, industry-standard JD for a clinical research role with clear tasks and regulatory expectations.
Must haves
- Bachelor's degree in a scientific or healthcare field
- 2+ years of clinical monitoring experience in Oncology trials
- Strong knowledge of GCP and ICH guidelines
- Proficiency in clinical trial management systems
- Ability and willingness to travel to clinical trial sites
Tools and skills
Nice to have: certified clinical research professional (ccrp), socra certification.
About the company
Established biopharmaceutical company, though not a global Tier-1 tech brand.